Judd Paul K, Kumar Renu B, Das Anath
Department of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, Minneapolis, MN 55455, USA.
Proc Natl Acad Sci U S A. 2005 Aug 9;102(32):11498-503. doi: 10.1073/pnas.0505290102. Epub 2005 Aug 2.
Type IV secretion is used by pathogenic microorganisms to transfer effector macromolecules to eukaryotic target cells. The VirB/D4 apparatus of Agrobacterium tumefaciens transfers DNA and proteins to plant cells. We postulated that the cell pole is the site of assembly of the A. tumefaciens type IV apparatus. Using immunofluorescence microscopy, we now demonstrate that 10 of the VirB proteins localized primarily to one cell pole and a macromolecular VirB complex is assembled at the pole. Neither the assembly of the complex nor polar localization of a VirB protein requires ATP utilization by the VirB ATPases. The requirement of other VirB proteins for the polar localization of at least six VirB proteins indicates an essential role of protein-protein interaction in polar targeting. Four proteins (VirB3, VirB4, VirB8, and VirB11) could target themselves to a cell pole independent of a VirB protein. We provide evidence that VirB6-VirB10 are the structural components of the type IV apparatus. Using strains that express defined subsets of the virB genes, we demonstrate that VirB7-VirB10 are the minimum components sufficient for the assembly of a polar VirB complex. VirB6 associates with this complex to form the type IV secretion apparatus. VirB8 functions as the assembly factor and targets the apparatus to the cell pole.
IV型分泌系统被致病微生物用于将效应大分子转移到真核靶细胞。根癌土壤杆菌的VirB/D4装置将DNA和蛋白质转移到植物细胞。我们推测细胞极是根癌土壤杆菌IV型装置的组装位点。利用免疫荧光显微镜,我们现在证明10种VirB蛋白主要定位于一个细胞极,并且一个大分子VirB复合物在该极组装。复合物的组装和VirB蛋白的极性定位都不需要VirB ATP酶利用ATP。其他VirB蛋白对至少六种VirB蛋白极性定位的需求表明蛋白质-蛋白质相互作用在极性靶向中起重要作用。四种蛋白(VirB3、VirB4、VirB8和VirB11)可以独立于VirB蛋白将自身靶向细胞极。我们提供证据表明VirB6-VirB10是IV型装置的结构成分。利用表达virB基因特定子集的菌株,我们证明VirB7-VirB10是组装极性VirB复合物所需的最小成分。VirB6与该复合物结合形成IV型分泌装置。VirB8作为组装因子,将该装置靶向细胞极。